ENST00000327047.6:c.225G>C
MANE Select
|
ENSP00000322280.1:p.Gly75=
|
|
ENST00000468836.2:c.201G>C
|
ENSP00000419892.2:p.Gly67=
|
|
ENST00000644099.1:c.66G>C
|
ENSP00000494762.1:p.Gly22=
|
|
ENST00000645441.1:c.67G>C
|
|
|
ENST00000327047.5:c.225G>C
|
ENSP00000322280.1:p.Gly75=
|
|
ENST00000328863.8:c.225G>C
|
ENSP00000329158.4:p.Gly75=
|
|
ENST00000468836.1:c.-176G>C
|
ENSP00000419892.1:n.-176G>C
|
|
ENST00000472224.1:n.231G>C
|
|
|
NM_001195794.1:c.225G>C , LRG_700t1:c.225G>C
|
NP_001182723.1:p.Gly75=
|
|
NM_001256819.1:c.225G>C
|
NP_001243748.1:p.Gly75=
|
|
NM_174878.2:c.225G>C
|
NP_777367.1:p.Gly75=
|
|
NR_046380.2:n.516G>C
|
|
|
XR_924167.1:n.537G>C
|
|
|
NM_001256819.2:c.225G>C
|
NP_001243748.1:p.Gly75=
|
|
NM_174878.3:c.225G>C
MANE Select
|
NP_777367.1:p.Gly75=
|
|
NR_046380.3:n.244G>C
|
|
|